Advin Biotech
United Statesfrom the FDA registration address FDA FEI 3010934853
- Devices
- 454
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Advin Biotech makes
Advin Biotech produces multiple drugs of abuse in vitro diagnostic (IVD) kits, rapid immunoconcentration tests (ICT), and clinical tests, as well as SARS-CoV-2 antigen IVD kits, rapid ICT tests, and self-testing kits.
The company's devices are classified as Class II, N, and U, and are listed in the FDA Unique Device Identification (UDI) registry. Advin Biotech is based in the US.
Catalogue
Search and filter all 454 devicesShowing 1-50 of 454
Company details
- FDA FEI number
- 3010934853
- Address
- 10140 Mesa Rim Rd., Unit 1, San Diego, CA, 92121
Frequently asked questions
How many devices does Advin Biotech have in the registry?
The registry currently lists 454 devices for Advin Biotech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Advin Biotech's devices?
Among its 50 most recently registered devices, Advin Biotech has devices listed in FDA GUDID (50 devices).
What risk classes do Advin Biotech's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Advin Biotech's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Advin Biotech in the registry?
The most recently registered devices listed for Advin Biotech include MYM Multi-Drug Urine Test Dipcard 1, QuikTox ULTRA DIP 1, QuikTox ULTRA CUP 1 and Multi-Drug Screen Test Cup 1.